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rs794728619

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728619(A;C)
Make rs794728619(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64808024
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728619
ebirs794728619
HLIrs794728619
Exacrs794728619
Varsomers794728619
Maprs794728619
PheGenIrs794728619
hapmaprs794728619
1000 genomesrs794728619
hgdprs794728619
ensemblrs794728619
gopubmedrs794728619
geneviewrs794728619
scholarrs794728619
googlers794728619
pharmgkbrs794728619
gwascentralrs794728619
openSNPrs794728619
23andMers794728619
23andMe allrs794728619
SNP Nexus

SNPshotrs794728619
SNPdbers794728619
MSV3drs794728619
GWAS Ctlgrs794728619
Max Magnitude0
ClinVar
Risk rs794728619(C;C)
Alt rs794728619(C;C)
Reference rs794728619(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575496T>G
CLNSRC
CLNACC RCV000182407.1,